Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11070921	0.86[CHB][hapmap]
rs11070935	0.90[ASN][1000 genomes]
rs12101773	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16965313	0.82[ASN][1000 genomes]
rs16965329	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs16965332	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1899739	0.80[ASN][1000 genomes]
rs2165989	0.80[ASN][1000 genomes]
rs2414187	0.83[ASN][1000 genomes]
rs2414215	0.85[ASN][1000 genomes]
rs2440331	0.81[ASN][1000 genomes]
rs2456520	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28758654	0.82[ASN][1000 genomes]
rs61262002	0.82[ASN][1000 genomes]
rs61588331	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62023539	0.89[ASN][1000 genomes]
rs7163077	0.82[ASN][1000 genomes]
rs7163093	0.82[ASN][1000 genomes]
rs7169953	0.82[ASN][1000 genomes]
rs73413458	0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2579232	chr15:53230986-53232223	Inactive region	TF binding region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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